Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside Volume Assessment.
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: In-person VExUS Training Program, Remote VExUS Training Program, No intervention.
- Кому может быть актуально
- Состояния в реестре: Acute Heart Failure (AHF), Fluid Over-load, Congestion, Congestion, Venous. Базовые параметры: Без ограничений · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Швейцария
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Training Medical Residents in the Use of the Venous Excess UltraSound (VExUS) Score for Bedside Volume Assessment: a Randomized Controlled Trial
Обзор
This randomized controlled trial evaluates the effectiveness of two training approaches (in-person versus remote) for teaching medical residents to apply the Venous Excess Ultrasound (VExUS) score for bedside volume assessment in patients with acute heart failure. Resident performance will be compared to that of expert physicians certified in abdominal and duplex sonography.
Подробное описание
Accurate assessment of volume status is essential in managing acute heart failure but remains challenging in clinical practice. The VExUS score is a validated ultrasound-based tool integrating inferior vena cava diameter and Doppler assessment of hepatic, portal, and intrarenal veins.
This single-center randomized controlled trial compares two training modalities (in-person vs. remote) in medical residents with basic ultrasound skills. Participants will be randomized 1:1 to either training method and compared to a control group of expert physicians.
Primary outcomes include ultrasound image quality assessed using a standardized 100-point score. Secondary outcomes include time to acquisition, VExUS scoring accuracy, self-confidence, and acceptability of training methods.
Вмешательства
- Поведенческое In-person VExUS Training Program
In-person training consisting of a 1-hour theoretical introduction followed by a 3-hour supervised hands-on ultrasound training session focusing on acquisition and interpretation of the VExUS score. - Поведенческое Remote VExUS Training Program
Remote training consisting of an e-learning module followed by independently performed ultrasound examinations with asynchronous expert feedback (via phone or email). - Другое No intervention
SGUM-certified physicians performing VExUS examinations as expert reference standard.
Первичные конечные точки
- Ultrasound Image Quality Score [Срок оценки: From training until 6 months after completion of training]
Вторичные конечные точки (5)
- Time for Image Acquisition and Interpretation [Срок оценки: From training until 6 months after completion of training]
- Change in self-confidence in performing VExUS assessment [Срок оценки: From baseline (before training) to immediately after completion of training]
- Acceptability of the program (quantitative assessment) [Срок оценки: Immediately after completion of training and during the outcome assessment period (within 2 months after training)]
- VEXUS score [Срок оценки: From training until 6 months after completion of training]
- Acceptability of the program (qualitative assessment) [Срок оценки: Immediately after completion of training and during the outcome assessment period (within 2 months after training)]
Критерии участия
Критерии включения
- Medical residents in general internal medicine
- Basic ultrasound skills (POCUS component 1 or ≥200 scans)
- Working at study site during study period
Критерии исключения
- SGUM certification in abdominal ultrasound
- Advanced duplex ultrasound experience
- Prior vascular/duplex training
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Простое слепое
- Основная цель
- Диагностика
Центры проведения
Швейцария · 1 центр
- Inselspital — Bern
Идентификаторы
NCT: NCT07541768 · VEXUS Teaching